ਜਾਂ ਸੰਬੰਧਿਤ ਜਾਂ ਸ਼ਾਮਲ ਗੋਨਾਡੋਟ੍ਰੋਪਿਨ,

gonadotropic's Usage Examples:

conditions termed hypogonadotropic hypogonadism.

Under regulation by gonadotropic hormones, ovarian follicles mature and estrogen secretions exert their biggest influence.

hypogonadotropic hypogonadism Familial male-limited precocious puberty (or LH oversensitivity) Follicle-stimulating hormone insensitivity Gonadotropin-releasing.

The condition manifests itself as isolated hypogonadotropic hypogonadism (IHH), presenting with symptoms such as delayed, reduced, or absent puberty.

Hypothalamic disorders result from a deficiency in the release of gonadotropic releasing hormone (GnRH), while pituitary gland disorders are due to.

Equine chorionic gonadotropin (acronym given as eCG but not to be confused with ECG) is a gonadotropic hormone produced in the chorion of pregnant mares.

The condition manifests itself as hypergonadotropic hypogonadism (decreased or lack of production of sex steroids by the gonads despite.

These gonadotropic hormones lead to sexual maturation and gametogenesis.

Luteinizing hormone (LH, also known as lutropin and sometimes lutrophin) is a hormone produced by gonadotropic cells in the anterior pituitary gland.

To distinguish it from other forms of hypogonadotropic hypogonadism, Kallmann syndrome has the additional.

characterized by loss of olfactory bulbs and GnRH secretion leading to anosmia and hypothalamic hypogonadotropic hypogonadism.

Defects in this gene are a cause of hypogonadotropic hypogonadism (HH).

Hypogonadotropic hypogonadism (HH), is due to problems with either the hypothalamus or pituitary gland affecting the hypothalamic-pituitary-gonadal axis.